Jiedu Fang inhibits hypoxia-induced angiogenesis in hepatocellular carcinoma by targeting Aurora A/STAT3/IL-8 signaling pathway

血管生成 肝细胞癌 癌症研究 信号转导 医学 机制(生物学) 肝癌 新生血管 药理学 信号通路 信号通路 刺猬信号通路
作者
Maofeng Zhong,Yujun Luo,Yu-yu Guo,Shuang Xiang,Wanfu Lin
出处
期刊:Journal of Integrative Medicine [Elsevier BV]
卷期号:23 (6): 683-693 被引量:1
标识
DOI:10.1016/j.joim.2025.09.002
摘要

OBJECTIVE: Angiogenesis is a critical target for hepatocellular carcinoma (HCC) treatment. The previous studies indicated that Jiedu Fang (JDF) could inhibit hypoxia-induced angiogenesis through interleukin-8 (IL-8). Therefore, the present study further explores the mechanisms behind JDF's inhibition of HCC angiogenesis. METHODS: Angiogenesis was assessed with the capillary-like tube formation assay in vitro and the matrigel plug angiogenesis assay in vivo. A liver cancer-related gene set and genes associated with angiogenesis and the hypoxic microenvironment were analyzed using a bioinformatics platform. Real-time reverse transcription-polymerase chain reaction and Western blotting assays were used to assess the targeted mRNA and protein levels, respectively. The Transwell assay was used to assess the migration and invasion potential of EA.hy 926 cells. The orthotopic tumor xenograft model was established, and immunohistochemistry and immunofluorescence assays were used to detect cluster of differentiation 31 and angiopoietin 2 expression, while an enzyme-linked immunosorbent assay was used to detect vascular endothelial growth factor and IL-8 protein levels. RESULTS: In vitro and in vivo assays showed that IL-8 promoted angiogenesis, and JDF could antagonize this effect. Bioinformatics analysis indicated that aurora kinase A (Aurora A) was an important candidate, which can promote IL-8 expression through activation of signal transducer and activator of transcription 3 (STAT3). The overexpression of Aurora A increased IL-8 secretion and promoted HCC migration, invasion, and angiogenesis, which was partly inhibited by JDF. Such effects were validated by in vivo assays. Further validation using the STAT3 inhibitor S3I-201 demonstrated that STAT3 was regulated by Aurora A. CONCLUSION: JDF exhibits efficacy in reducing hypoxia-induced angiogenesis in HCC through a mechanism involving the Aurora A/STAT3/IL-8 signaling pathway. Therefore, JDF holds promise as a potential therapeutic approach for targeting HCC angiogenesis. Please cite this article as: Zhong MF, Luo YJ, Guo YY, Xiang S, Lin WF. Jiedu Fang inhibits hypoxia-induced angiogenesis in hepatocellular carcinoma by targeting Aurora A/STAT3/IL-8 signaling pathway. J Integr Med. 2025; 23(6):683-693.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
科研通AI6.4应助兔子大王采纳,获得10
刚刚
领导范儿应助起风了采纳,获得10
1秒前
悦耳的涫发布了新的文献求助10
1秒前
swg发布了新的文献求助10
2秒前
3秒前
Azlne发布了新的文献求助20
3秒前
4秒前
深情安青应助松饼采纳,获得10
5秒前
不必要再讨论适合与否完成签到,获得积分0
5秒前
5秒前
林木木应助侯mm采纳,获得10
5秒前
香蕉觅云应助心芷采纳,获得10
6秒前
xxzxg_nono完成签到,获得积分10
7秒前
传奇3应助晓湫采纳,获得10
7秒前
zzz发布了新的文献求助10
7秒前
例外完成签到,获得积分10
7秒前
sheep发布了新的文献求助10
8秒前
9秒前
酷波er应助Summerrrrui采纳,获得10
9秒前
bq完成签到 ,获得积分10
9秒前
简体了再说完成签到,获得积分20
9秒前
热爱生活关注了科研通微信公众号
9秒前
花砸完成签到,获得积分10
10秒前
10秒前
chaijy87完成签到,获得积分10
10秒前
10秒前
万能图书馆应助莹莹啊采纳,获得10
11秒前
牧青发布了新的文献求助30
11秒前
12秒前
阳阳秋完成签到,获得积分10
13秒前
大道要熬完成签到,获得积分10
13秒前
sagitar应助nature采纳,获得20
13秒前
14秒前
14秒前
纯真蓝完成签到,获得积分20
14秒前
NexusExplorer应助sheep采纳,获得10
15秒前
章鱼发布了新的文献求助10
15秒前
白桃完成签到 ,获得积分10
15秒前
wang完成签到,获得积分10
17秒前
17秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
HYDROLYSE ACIDE DE QUELQUES DIOXASPIROCYCLANES 1314
Essentials of Carbohydrate Chemistry and Biochemistry, 4th Edition 800
Navigating Normative Orders. Interdisciplinary Perspectives 800
1 Peter and Christ's Descent to the Dead in Its Early Christian Reception 700
Organizational Behavior 510
Management and the Arts 510
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 内科学 物理 复合材料 催化作用 细胞生物学 无机化学 光电子学 物理化学 电极 基因
热门帖子
关注 科研通微信公众号,转发送积分 7746011
求助须知:如何正确求助?哪些是违规求助? 9293895
关于积分的说明 20222561
捐赠科研通 7325687
什么是DOI,文献DOI怎么找? 3308029
关于科研通互助平台的介绍 2459990
邀请新用户注册赠送积分活动 2319466